Product image of Noliprel A (Indapamide, Perindopril Arginine) supplied by GNH India

Noliprel A

Active Ingredient:
Indapamide, Perindopril Arginine
Origin:
EU

Noliprel A (Indapamide, Perindopril Arginine)

Indapamide and Perindopril arginine, the active ingredients in Noliprel A, are an ACE inhibitor and a thiazide‑like diuretic presented as an oral tablet for systemic use. They are prescribed to manage hypertension in adult patients.

GNH India supplies Noliprel A as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Anpharm Przedsiębiorstwo Farmaceutyczne Spółka Akcyjna

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Indications & Clinical Uses

Noliprel A is used in the management of hypertension, a condition characterized by elevated systemic arterial pressure.

  • Hypertension: lowers systolic and diastolic blood pressure to reduce cardiovascular risk.
  • Essential hypertension: provides consistent blood pressure control when monotherapy is insufficient.
  • High‑risk hypertensive patients: contributes to overall risk reduction for stroke and myocardial infarction.

How It Works

  • Indapamide acts on the distal renal tubule to inhibit sodium reabsorption, promoting diuresis and reducing plasma volume. Perindopril arginine blocks the angiotensin‑converting enzyme, decreasing formation of angiotensin II, which leads to vasodilation, reduced aldosterone secretion, and lowered systemic vascular resistance, together achieving blood pressure reduction.

Side Effects

Noliprel A may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Dizziness or light‑headedness
  • Headache
  • Persistent dry cough
  • Fatigue or weakness
  • Increased urination
  • Electrolyte disturbances (e.g., low potassium)

Serious or Rare Side Effects

  • Angioedema (swelling of face, lips, tongue)
  • Severe hypotension
  • Acute renal impairment
  • Hyperkalemia
  • Neutropenia or agranulocytosis
  • Hepatic dysfunction

Precautions & Warnings

Before initiating Noliprel A, several safety considerations should be observed.

  • Blood pressure monitoring: ensure adequate control and avoid excessive drops.
  • Renal function assessment: check serum creatinine and eGFR regularly.
  • Electrolyte balance: monitor potassium and sodium levels, especially in patients on other diuretics.
  • Hepatic impairment: use caution in patients with severe liver disease.
  • Diabetes management: watch for changes in blood glucose control.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Noliprel A can interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Potassium‑sparing diuretics or supplements: risk of hyperkalemia.
  • Aliskiren in diabetic patients: may cause renal dysfunction.
  • Lithium: increased lithium levels and toxicity.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may blunt antihypertensive effect and impair renal function.
  • Other ACE inhibitors or ARBs: additive risk of angioedema and hypotension.

Moderate Interactions (Monitor Closely)

  • Other antihypertensives (beta‑blockers, calcium channel blockers): may require dose adjustment.
  • Antidiabetic agents: possible enhancement of hypoglycaemic effect.
  • High‑dose aspirin: may affect renal perfusion.
  • Warfarin: potential alteration of INR values.
  • Corticosteroids: may increase sodium retention and counteract diuretic effect.

Frequently Asked Questions

Noliprel A is a prescription medication that combines indapamide and perindopril arginine to treat hypertension. By lowering elevated blood pressure, it helps reduce the risk of cardiovascular events such as stroke and heart attack in adult patients.

Indapamide increases urine output by blocking sodium reabsorption in the distal renal tubule, which reduces fluid volume. Perindopril arginine inhibits the angiotensin‑converting enzyme, decreasing angiotensin II production and causing vasodilation. Together they lower systemic vascular resistance and blood pressure.

The appropriate dose of Noliprel A is determined by the prescribing healthcare professional based on the individual’s medical condition, response to therapy, and other medications. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

The safety of Noliprel A in pregnancy or while breastfeeding has not been fully established. Healthcare providers usually avoid prescribing ACE inhibitors and thiazide‑like diuretics during the first trimester and advise caution throughout pregnancy and lactation. Discuss any concerns with a qualified clinician.

To order Noliprel A, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Noliprel A combines a thiazide‑like diuretic with an ACE inhibitor, offering dual mechanisms that can be more effective than monotherapy for patients whose blood pressure is not controlled with a single agent. Compared with separate tablets, the fixed‑dose combination may improve adherence and simplify dosing.

Noliprel A tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the container tightly closed and out of reach of children.

Noliprel A is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a full glass of water and do not crush or chew it unless instructed otherwise.

Serious risks include angioedema, severe hypotension, acute renal impairment, and hyperkalemia. Patients should seek immediate medical attention if they experience swelling of the face or throat, sudden dizziness, reduced urine output, or muscle weakness.

Noliprel A is contraindicated in individuals with a known hypersensitivity to indapamide, perindopril arginine, or any component of the formulation, as well as in patients with a history of angioedema related to ACE‑inhibitor therapy. It should also be avoided in severe renal or hepatic impairment unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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